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Effects of wheat straw mulching and wet treatment on soil improvement, greenhouse gas emission, nitrogen leaching, and vegetable yield 小麦秸秆覆盖加湿处理对土壤改良、温室气体排放、氮淋失和蔬菜产量的影响
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2025-01-03 DOI: 10.1016/j.hpj.2024.05.018
Zhiping Zhang, Jin Yan, Xueshuang Gao, Zijian Zheng, Li Xu, Zihui Zhu, Jiezeng Jiang, Minmin Miao
Plastic tunnels are a crucial tool used for intensive vegetable production in developing countries, however these tunnels have resulted in significant soil degradation. Another issue that the agriculture industry is facing is that an excess of crop straw is produced every year. This paper aims to combat both of these issues by combining them: to relieve soil degradation and consume crop straw, six treatments of three wheat straw quantities (0, 5,000 and 10 000 kg · hm−2) and two soil moisture levels (wet and submergence) were evaluated during two-month high-temperature summers to explore the possibility of applying straw mulching to improve degraded soil in plastic tunnels. Greenhouse gas emission and nitrogen leaching, which are two other significant problems with using intensive vegetable tunnels, were also investigated. Compared to the no straw mulching and wet treatment, the net global warming potential, available nitrogen, nitrogen leaching, and N2O emissions from subsequent crop fields decreased by 389.59%, 21.2%, 45.9%, and 41.5%, respectively. The soil-available phosphorus, available potassium, total nitrogen, total phosphorus, total potassium, organic carbon, microbial biomass carbon, microbial biomass nitrogen, activities of urease, sucrase, and acid phosphatase, and yields of cucumber and tomato increased by 2%, 79.6%, 75.3%, 51.4%, 92.5%, 32.8%, 122.1%, 152.5%, 103.9%, 102%, 88.6%, 19% and 13%, respectively, in the 10 000 kg straw and wet treatment. According to the 15N-site preference value, nitrification was the dominant pathway for N2O production in the field, and its contribution was enhanced by straw mulching and weakened by submergence. Considering all factors, no significant advantage was found for submergence compared with wet treatment, while treatment with 10 000 kg of straw showed remarkable improvement over the treatment with 5,000 kg of straw. We conclude that applying 10 000 kg of wheat straw in conjunction with the wet treatment during the summer fallow period has wide application potential to improve degraded soil, alleviate secondary salinization and nitrogen leaching, and consume crop straw without increasing net global warming potential.
塑料隧道是发展中国家蔬菜集约化生产的重要工具,但这些隧道造成了严重的土壤退化。农业面临的另一个问题是每年生产的农作物秸秆过剩。为了缓解土壤退化和消耗农作物秸秆,本研究在两个月的高温夏季评估了三种小麦秸秆量(0,5,000和10,000 kg·hm−2)和两种土壤水分水平(潮湿和淹没)的六种处理,以探索使用秸秆覆盖改善塑料隧道退化土壤的可能性。温室气体排放和氮淋失是集约化蔬菜隧道利用的另外两个主要问题。与无秸秆覆盖和湿处理相比,秸秆覆盖后农田的净全球变暖潜势、有效氮、氮淋溶和N2O排放量分别减少了389.59%、21.2%、45.9%和41.5%。土壤速效磷、速效钾、全氮、全磷、全钾、有机碳、微生物量碳、微生物量氮、脲酶、蔗糖酶和酸性磷酸酶活性以及黄瓜和番茄产量分别比施用1万kg秸秆和湿处理提高了2%、79.6%、75.3%、51.4%、92.5%、32.8%、122.1%、152.5%、103.9%、102%、88.6%、19%和13%。从15n位点的偏好值来看,硝化作用是田间N2O生产的主要途径,秸秆覆盖增强了其贡献,淹水削弱了其贡献。综合考虑各因素,浸泡处理与湿处理相比无显著优势,而10000 kg秸秆处理比5000 kg秸秆处理有显著改善。综上所述,在夏季休耕期施用10 000 kg小麦秸秆配合湿法处理具有改善退化土壤、缓解二次盐碱化和氮淋失、消耗秸秆而不增加全球净变暖潜势的广阔应用潜力。
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引用次数: 0
VvPIP1;1 plays a role in grape berry cracking by regulating water uptake vppip1;1通过调节水分吸收在葡萄果实开裂中起作用
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2025-01-03 DOI: 10.1016/j.hpj.2024.07.010
Jun Yu, Jia Li, Zhangfen Hong, Qing Zeng, Yizheng Fu, Rouxue Deng, Ke Xu, Zhenyu Huang, Mingtao Zhu
Fruit cracking is a persistent challenge for table grape growing. To investigate the mechanism of this disorder, a comprehensive two-year investigation was conducted to assess the fruit cracking percentage of 15 table grape (Vitis vinifera L.) varieties. Based on the findings, the cracking-susceptible variety ‘Xiangfei’ and the cracking-resistant variety ‘Zuijinxiang’ were selected for further study. Fruit growth curves for ‘Zuijinxiang’ and ‘Xiangfei’ were plotted based on fruit diameter and total soluble solids content, revealing that both varieties exhibited typical double-sigmoidal patterns that were highly similar. The period between 48 and 53 days after full bloom (DAFB) was identified as the critical phase for fruit cracking incidence. Furthermore, during the fruit cracking period, ‘Xiangfei’ fruit exhibited significantly higher water content and mesocarp cell area compared with those of ‘Zuijinxiang’. Applying aquaporin inhibitors (nano-silver) to ‘Xiangfei’ berries reduced fruit water uptake and cracking percentage, whereas applying aquaporin activators (forskolin) to ‘Zuijinxiang’ berries increased fruit water uptake and cracking percentage. Additionally, expression analysis of six genes associated with plasma membrane intrinsic proteins (PIPs) synthesis (VvPIP1;1, VvPIP1;2, VvPIP1;3, VvPIP2;1, VvPIP2;2, and VvPIP2;3) revealed that only the expression level of VvPIP1;1 was higher in ‘Zuijinxiang’ than in ‘Xiangfei’ during the fruit cracking period, whereas the expression levels of the other genes exhibited no significant difference between the two varieties. Transgenic overexpression of VvPIP1;1 in tomato resulted in increased fruit water content, enlarged mesocarp cell size, and enhanced fruit cracking percentage. These findings indicate that VvPIP1;1 plays a pivotal role in controlling grape berry cracking.
水果开裂是食用葡萄种植的一个持久的挑战。为了探讨这种病害的发生机制,对15个鲜食葡萄品种进行了为期两年的果实开裂率调查。在此基础上,选择易裂品种“香飞”和抗裂品种“醉金香”进行进一步研究。根据果实直径和总可溶性固形物含量绘制了‘醉金香’和‘香飞’的果实生长曲线,结果表明,这两个品种都表现出典型的双s型曲线,两者高度相似。结果表明,开花后48 ~ 53 d是果实开裂发生的关键时期。在果实开裂期,‘香飞’果实的含水量和中果皮细胞面积显著高于‘醉金香’。在“香飞”浆果上施用水通道蛋白抑制剂(纳米银)降低了果实的吸水率和开裂率,而在“醉金香”浆果上施用水通道蛋白活化剂(forskolin)提高了果实的吸水率和开裂率。此外,对6个与质膜内在蛋白(PIPs)合成相关的基因(VvPIP1;1, VvPIP1;2, VvPIP1;3, VvPIP2;1, VvPIP2;2, VvPIP2;3)的表达分析显示,在果实破裂期,只有VvPIP1;1在“醉金香”中的表达水平高于“湘非”,而其他基因的表达水平在两个品种之间无显著差异。在番茄中转基因过表达VvPIP1;1导致果实含水量增加,中果皮细胞大小增大,果实开裂率提高。这些发现表明,VvPIP1;1在控制葡萄果实开裂中起着关键作用。
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引用次数: 0
Application of an efficient adenine base editing system in developing Danshen (Salvia miltiorrhiza) dinitroaniline-resistant germplasm 高效腺嘌呤碱基编辑系统在丹参二硝基苯胺抗性种质开发中的应用
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-30 DOI: 10.1016/j.hpj.2024.08.007
Huanan Han, Ziwen Wu, Zaijie Zhang, Yusen Qu, Yingcan Wang, Pingping Wang, Changle Ma
Chinese herbal medicine Danshen (Salvia miltiorrhiza) has suggested therapeutic effects on cardiovascular and cerebrovascular diseases, inflammatory reactions and tumors, perhaps due to secondary metabolites, such as tanshinone. Danshen is sensitive to most broad-spectrum herbicides, thus it is a challenge to manage weeds during planting. Although CRISPR/Cas gene editing has been used to knock out important genes in Danshen, the more accurate base editing method has rarely been applied to this species. We developed an efficient adenine base editing system for Danshen and observed its editing effect in callus and transgenic plants. To demonstrate the efficacy of this technique, we generated several novel Danshen germplasms with mutant α-tubulins, some of which displayed resistance to a dinitroaniline herbicide, pendimethalin, in Danshen planting. We also found distinct effects of the different Danshen mutant tubulin homologues on dinitroaniline sensitivity, perhaps indicating a functional differentiation of the α-tubulin genes. Our work provides a new gene modification method for Danshen breeding, which might be extended to other medicinal plants.
中药丹参(丹参)被认为对心脑血管疾病、炎症反应和肿瘤有治疗作用,可能是由于其次生代谢产物,如丹参酮。丹参对大多数广谱除草剂敏感,因此在种植过程中对杂草进行治理是一个挑战。虽然CRISPR/Cas基因编辑已经被用于敲除丹参的重要基因,但更精确的碱基编辑方法很少应用于该物种。我们开发了一种高效的丹参腺嘌呤碱基编辑系统,并观察了其在愈伤组织和转基因植株上的编辑效果。为了证明该技术的有效性,我们在丹参种植中获得了几种具有α-微管蛋白突变体的新型丹参种质,其中一些对二硝基苯胺类除草剂戊二甲基灵具有抗性。我们还发现不同丹参突变体微管蛋白同源物对二硝基苯胺敏感性的不同影响,这可能表明α-微管蛋白基因的功能分化。本研究为丹参育种提供了一种新的基因修饰方法,可推广到其他药用植物中。
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引用次数: 0
GWAS-driven gene mining and genomic prediction of ornamental traits in flowering trees: A case study of Camellia japonica gwas驱动的开花树木观赏性状基因挖掘与基因组预测——以山茶为例
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-27 DOI: 10.1016/j.hpj.2024.05.017
Menglong Fan, Xiaojuan Wei, Zhixin Song, Ying Zhang, Xinlei Li, Zhenyuan Sun
Floral traits largely determine the ornamental value of horticultural plants, while the long juvenile period of woody plants hinders the progress of the floral pattern and color breeding. The population genetic variations in the floral characters of cultivated camellias are far less well understood and applied. Here, we investigated genetic architecture and genome prediction of the floral pattern and color in Camelia japonica. Seven anthocyanins were identified in 200 camellia cultivars using an ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) approach. The content and proportional changes in Cy3G and Cy3GEpC were identified as the main cause of the color change. A total of 2 072 667 SNPs were identified, the population structure analysis revealed frequent gene infiltration among the cultivars. A genome-wide association study (GWAS) and the transcriptome analysis identified 163 and 46 shared genes significantly associated with the floral color and pattern, respectively. Furthermore, Support Vector Machine (SVM) regression with linear kernel and the top 1000 and 10 000 GWAS associated markers achieved the highest prediction accuracy for a petal number of 94 %, and anthocyanin content of 95 %. Our study provides novel insight into the genetic basis of floral characters and confirms the feasibility of using machine learning and GWAS markers to predict floral traits, which will accelerate the ornamental molecular breeding of C. japonica.
花性状在很大程度上决定了园艺植物的观赏价值,而木本植物幼龄过长阻碍了花色育种的进展。栽培山茶花性状的群体遗传变异还远远没有得到很好的理解和应用。本文研究了山茶(Camelia japonica)花型和花色的遗传结构和基因组预测。采用超高效液相色谱-质谱联用技术,从200个茶花品种中鉴定出7种花青素。Cy3G和Cy3GEpC的含量和比例变化是导致颜色变化的主要原因。共鉴定出2 072 667个snp,群体结构分析显示品种间基因浸润频繁。全基因组关联研究(GWAS)和转录组分析分别鉴定出163个和46个与花的颜色和图案显著相关的共享基因。利用线性核和前1000个和前10000个GWAS相关标记进行支持向量机(SVM)回归,对花瓣数和花青素含量的预测准确率最高,分别为94%和95%。本研究为花性状的遗传基础提供了新的认识,并证实了利用机器学习和GWAS标记预测花性状的可行性,这将加速粳稻观赏分子育种的发展。
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引用次数: 0
Strigolactone as a potential target for improving abiotic stress tolerance in horticultural crops 独角麦内酯作为提高园艺作物非生物抗逆性的潜在靶点
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-27 DOI: 10.1016/j.hpj.2024.06.011
Wanni Wang, Yulin Fang, Yanlun Ju
Crop yield and quality are affected by abiotic stresses such as drought, low and high temperature, salinity, and heavy metals, which threaten the survival of human beings and the development of industry. As a new plant hormone derived from carotenoid, strigolactone (SL) is produced in the roots of plants. It was first reported that SL can induce seed germination of root-parasitic plants. In recent years, it has been shown that strigolactone plays a regulatory role in plant response to abiotic stresses. By eliminating oxidative stress caused by reactive oxygen species, it can potentially increase photosynthetic rate, chlorophyll content, and thus enhance plant drought resistance. Transcriptome studies have explored signal transduction, antioxidant enzyme activity, transcription factors, and expression of stress-and metabolism-related genes induced by extrinsic strigolactone in plants, the effects of strigolactone on plant growth and development have been preliminarily determined, but the studies on inducing crop tolerance to abiotic stresses are still unknown. In this review, the physiological and molecular aspects of the induction of the response to stress in horticultural crops by strigolactone were reviewed. It is important to improve the tolerance and productivity of horticultural crops under abiotic stress.
农作物产量和品质受到干旱、低温、高温、盐碱、重金属等非生物胁迫的影响,威胁着人类的生存和工业的发展。独角曲内酯(SL)是一类从类胡萝卜素中衍生出来的新型植物激素,产生于植物的根部。SL可以诱导根寄生植物种子萌发,这是首次报道。近年来,研究表明独角麦内酯在植物对非生物胁迫的响应中起调节作用。通过消除活性氧引起的氧化应激,有可能提高光合速率和叶绿素含量,从而增强植物抗旱性。转录组研究探索了外源独角麦内酯诱导植物的信号转导、抗氧化酶活性、转录因子以及胁迫代谢相关基因的表达,初步确定了独角麦内酯对植物生长发育的影响,但诱导作物耐受非生物胁迫的研究尚不清楚。本文从生理和分子两个方面综述了独角麦内酯诱导园艺作物逆境响应的研究进展。提高园艺作物对非生物胁迫的耐受性和生产力具有重要意义。
{"title":"Strigolactone as a potential target for improving abiotic stress tolerance in horticultural crops","authors":"Wanni Wang, Yulin Fang, Yanlun Ju","doi":"10.1016/j.hpj.2024.06.011","DOIUrl":"https://doi.org/10.1016/j.hpj.2024.06.011","url":null,"abstract":"Crop yield and quality are affected by abiotic stresses such as drought, low and high temperature, salinity, and heavy metals, which threaten the survival of human beings and the development of industry. As a new plant hormone derived from carotenoid, strigolactone (SL) is produced in the roots of plants. It was first reported that SL can induce seed germination of root-parasitic plants. In recent years, it has been shown that strigolactone plays a regulatory role in plant response to abiotic stresses. By eliminating oxidative stress caused by reactive oxygen species, it can potentially increase photosynthetic rate, chlorophyll content, and thus enhance plant drought resistance. Transcriptome studies have explored signal transduction, antioxidant enzyme activity, transcription factors, and expression of stress-and metabolism-related genes induced by extrinsic strigolactone in plants, the effects of strigolactone on plant growth and development have been preliminarily determined, but the studies on inducing crop tolerance to abiotic stresses are still unknown. In this review, the physiological and molecular aspects of the induction of the response to stress in horticultural crops by strigolactone were reviewed. It is important to improve the tolerance and productivity of horticultural crops under abiotic stress.","PeriodicalId":13178,"journal":{"name":"Horticultural Plant Journal","volume":"27 1","pages":""},"PeriodicalIF":5.7,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142929187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ALA up-regulated PpWRKY18 to enhance freezing tolerance of nectarine pistils ALA上调PpWRKY18,提高油桃雌蕊的抗冻能力
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-27 DOI: 10.1016/j.hpj.2024.09.004
Zhouyu Yuan, Jianting Zhang, Longbo Liu, Liuzi Zhang, Xing Gan, Yan Zhong, Liangju Wang
5-Aminolevulinic acid (ALA) is a natural plant growth regulator that promotes plant freezing tolerance. The WRKY family consists of plant-specific transcription factors (TFs) associated with abiotic stress responses. Up to now, whether WRKYs are involved in ALA-induced plant freezing tolerance and the underlying mechanism is not clear. In this study, we found that pretreatment with 50 mg·L−1 ALA one week earlier significantly increased the freezing tolerance of nectarine (Prunus persica var. nectarina) pistils with higher antioxidant enzyme activity and osmotic solutes when the floral twigs were stressed by −3 °C for 6 h. ALA also enhanced the expression of PpWRKY18, PpCBF1, PpCOR1, and several genes encoding antioxidant enzymes (such as superoxide dismutase, peroxidase, and catalase) and pyrroline-5-carboxylate synthase (P5CS). When PpWRKY18 was overexpressed in tobacco, the transgenic plants exhibited greater freezing tolerance, which was further promoted by exogenous ALA. Y2H, Pull-down, BiFC, and LCI analyses revealed that PpWRKY18 interacts with PpCBF1, promoting the latter transcriptional activity. Additionally, Y1H experiments showed that PpWRKY18 directly binds to the promoter of PpPOD41 while PpCBF1 binds to the promoters of PpP5CS1 and PpCOR1, activating the target gene expressions. Furthermore, we established a yeast library using the promoter of PpWRKY18 as the bait to screen the upstream regulatory factors. By library screening, Y1H, DLR, and EMSA, we found that PpC3H37, a zinc finger protein, was responsive to chilling and ALA treatment, and as a transcription factor, it activated PpWRKY18 expression by directly binding to the promoter. Taken together, we reveal a regulatory network where ALA induces upregulation of PpC3H37 expression, which positively regulates PpWRKY18 expression. Subsequently, the regulatory pathway diverges into two branches. The first is CBF-dependent, where PpCBF1 interacts with PpWRKY18, binding the promoters of PpP5CS1 and PpCOR1. The second is CBF-independent, where PpWRKY18 directly binds the promoter of PpPOD41 to upregulate the gene expression and increase the antioxidant enzyme activity and freezing tolerance. These findings provide a novel insight of the mechanism of ALA in regulating the cold hardiness of nectarine pistil.
5-氨基乙酰丙酸(ALA)是促进植物抗冻性的天然植物生长调节剂。WRKY家族由与非生物胁迫反应相关的植物特异性转录因子(TFs)组成。到目前为止,WRKYs是否参与ala诱导的植物抗冻性及其机制尚不清楚。本研究发现,当花枝在−3°C环境下胁迫6 h时,提前1周处理50 mg·L−1 ALA可显著提高油桃雌蕊的抗冻性,并提高其抗氧化酶活性和渗透溶质。ALA还可提高PpWRKY18、PpCBF1、PpCOR1以及一些编码抗氧化酶(如超氧化物歧化酶、过氧化物酶、过氧化氢酶等)基因的表达。过氧化氢酶)和吡咯-5-羧酸合成酶(P5CS)。当PpWRKY18在烟草中过表达时,转基因植株表现出更强的抗冻能力,外源ALA进一步促进了抗冻能力的增强。Y2H、Pull-down、BiFC和LCI分析显示PpWRKY18与PpCBF1相互作用,促进后者的转录活性。此外,Y1H实验表明PpWRKY18直接结合PpPOD41的启动子,PpCBF1结合PpP5CS1和PpCOR1的启动子,激活靶基因表达。此外,我们以PpWRKY18启动子为诱饵,建立酵母文库,筛选上游调控因子。通过文库筛选、Y1H、DLR和EMSA,我们发现锌指蛋白PpC3H37对低温和ALA处理有响应,并且作为转录因子,它通过直接结合启动子激活PpWRKY18的表达。综上所述,我们揭示了一个ALA诱导PpC3H37表达上调的调控网络,其正向调节PpWRKY18的表达。随后,调控途径分化为两个分支。第一种是cbf依赖性的,其中PpCBF1与PpWRKY18相互作用,结合PpP5CS1和PpCOR1的启动子。第二种是不依赖cbf的,PpWRKY18直接结合PpPOD41的启动子上调基因表达,提高抗氧化酶活性和抗冻能力。这些发现为ALA调控油桃雌蕊抗寒性的机制提供了新的视角。
{"title":"ALA up-regulated PpWRKY18 to enhance freezing tolerance of nectarine pistils","authors":"Zhouyu Yuan, Jianting Zhang, Longbo Liu, Liuzi Zhang, Xing Gan, Yan Zhong, Liangju Wang","doi":"10.1016/j.hpj.2024.09.004","DOIUrl":"https://doi.org/10.1016/j.hpj.2024.09.004","url":null,"abstract":"5-Aminolevulinic acid (ALA) is a natural plant growth regulator that promotes plant freezing tolerance. The WRKY family consists of plant-specific transcription factors (TFs) associated with abiotic stress responses. Up to now, whether WRKYs are involved in ALA-induced plant freezing tolerance and the underlying mechanism is not clear. In this study, we found that pretreatment with 50 mg·L<ce:sup loc=\"post\">−1</ce:sup> ALA one week earlier significantly increased the freezing tolerance of nectarine (<ce:italic>Prunus persica</ce:italic> var. <ce:italic>nectarina</ce:italic>) pistils with higher antioxidant enzyme activity and osmotic solutes when the floral twigs were stressed by −3 °C for 6 h. ALA also enhanced the expression of <ce:italic>PpWRKY18</ce:italic>, <ce:italic>PpCBF1</ce:italic>, <ce:italic>PpCOR1</ce:italic>, and several genes encoding antioxidant enzymes (such as superoxide dismutase, peroxidase, and catalase) and pyrroline-5-carboxylate synthase (P5CS). When <ce:italic>PpWRKY18</ce:italic> was overexpressed in tobacco, the transgenic plants exhibited greater freezing tolerance, which was further promoted by exogenous ALA. Y2H, Pull-down, BiFC, and LCI analyses revealed that PpWRKY18 interacts with PpCBF1, promoting the latter transcriptional activity. Additionally, Y1H experiments showed that PpWRKY18 directly binds to the promoter of <ce:italic>PpPOD41</ce:italic> while PpCBF1 binds to the promoters of <ce:italic>PpP5CS1</ce:italic> and <ce:italic>PpCOR1</ce:italic>, activating the target gene expressions. Furthermore, we established a yeast library using the promoter of <ce:italic>PpWRKY18</ce:italic> as the bait to screen the upstream regulatory factors. By library screening, Y1H, DLR, and EMSA, we found that PpC3H37, a zinc finger protein, was responsive to chilling and ALA treatment, and as a transcription factor, it activated <ce:italic>PpWRKY18</ce:italic> expression by directly binding to the promoter. Taken together, we reveal a regulatory network where ALA induces upregulation of <ce:italic>PpC3H37</ce:italic> expression, which positively regulates <ce:italic>PpWRKY18</ce:italic> expression. Subsequently, the regulatory pathway diverges into two branches. The first is CBF-dependent, where PpCBF1 interacts with PpWRKY18, binding the promoters of <ce:italic>PpP5CS1</ce:italic> and <ce:italic>PpCOR1</ce:italic>. The second is CBF-independent, where PpWRKY18 directly binds the promoter of <ce:italic>PpPOD41</ce:italic> to upregulate the gene expression and increase the antioxidant enzyme activity and freezing tolerance. These findings provide a novel insight of the mechanism of ALA in regulating the cold hardiness of nectarine pistil.","PeriodicalId":13178,"journal":{"name":"Horticultural Plant Journal","volume":"48 1","pages":""},"PeriodicalIF":5.7,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142929190","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A novel bHLH transcription factor LlbHLH12 negatively regulates anthocyanin biosynthesis during Lycoris longituba petal development 一种新的bHLH转录因子LlbHLH12在石蒜花瓣发育过程中负调控花青素的生物合成
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-21 DOI: 10.1016/j.hpj.2024.07.009
Keyi Feng, Hongyan Tan, Ling Zhou, Tingting Shi, Lianggui Wang, Yuanzheng Yue, Xiulian Yang
Flower color is an essential trait in ornamental plant breeding. Lycoris longituba is a popular ornamental plant native to central eastern China. The decrease in anthocyanin accumulation causes L. longituba petal color fading during flower development, which considerably affects the ornamental value of L. longituba. However, mechanisms underlying anthocyanin biosynthesis inhibition during L. longituba petal development remain unclear. In this study, three LlDFR genes were confirmed to be involved in anthocyanin biosynthesis and LlDFRc exerted the strongest promoting effect on anthocyanin accumulation. According to the correlation analysis results, LlbHLH12 exhibited the strongest negative correlation with LlDFRc. Quantitative real-time PCR analysis showed that LlbHLH12 was highly expressed during the medium bud and full bloom stages of flower development. LlbHLH12 was identified as a member of subgroup XII of bHLH transcription factor family. Subcellular localization and transcriptional activation ability assay revealed that LlbHLH12 was located in the nucleus without transcriptional activation activity. Overexpression of LlbHLH12 in Nicotiana tabacum and L. longituba inhibited anthocyanin accumulation by suppressing the expression of anthocyanin biosynthetic pathway genes. Furthermore, yeast one-hybrid, dual-luciferase, and β-glucuronidase activity assays showed that LlbHLH12 directly bound to the promoters of LlPAL and LlDFRc and suppressed their expression to inhibit anthocyanin biosynthesis. Overall, our study identified a novel bHLH repressor negatively regulating anthocyanin biosynthesis and provided new insights into the molecular mechanisms underlying color fading in L. longituba petals.
花色是观赏植物育种的重要性状。石蒜是一种流行的观赏植物,原产于中国中东部。花色素苷积累的减少导致花发育过程中花瓣变色,严重影响了花的观赏价值。然而,花青素生物合成抑制的机制在L. longitude花瓣发育中仍不清楚。本研究证实了3个LlDFR基因参与了花青素的生物合成,其中LlDFRc对花青素积累的促进作用最强。相关分析结果显示,LlbHLH12与LlDFRc负相关最强。实时荧光定量PCR分析显示,LlbHLH12在花发育的中芽期和盛花期高表达。LlbHLH12被鉴定为bHLH转录因子家族的XII亚群成员。亚细胞定位和转录激活能力分析表明,LlbHLH12位于细胞核内,无转录激活活性。LlbHLH12在烟叶和纵叶中过表达是通过抑制花青素合成途径基因的表达来抑制花青素积累的。此外,酵母单杂交、双荧光素酶和β-葡萄糖醛酸酶活性测定表明,LlbHLH12直接结合LlPAL和LlDFRc启动子并抑制其表达,从而抑制花青素的生物合成。总之,我们的研究发现了一种新的bHLH抑制因子负调控花青素的生物合成,并为纵向兰花瓣褪色的分子机制提供了新的见解。
{"title":"A novel bHLH transcription factor LlbHLH12 negatively regulates anthocyanin biosynthesis during Lycoris longituba petal development","authors":"Keyi Feng, Hongyan Tan, Ling Zhou, Tingting Shi, Lianggui Wang, Yuanzheng Yue, Xiulian Yang","doi":"10.1016/j.hpj.2024.07.009","DOIUrl":"https://doi.org/10.1016/j.hpj.2024.07.009","url":null,"abstract":"Flower color is an essential trait in ornamental plant breeding. <ce:italic>Lycoris longituba</ce:italic> is a popular ornamental plant native to central eastern China. The decrease in anthocyanin accumulation causes <ce:italic>L. longituba</ce:italic> petal color fading during flower development, which considerably affects the ornamental value of <ce:italic>L. longituba</ce:italic>. However, mechanisms underlying anthocyanin biosynthesis inhibition during <ce:italic>L. longituba</ce:italic> petal development remain unclear. In this study, three <ce:italic>LlDFR</ce:italic> genes were confirmed to be involved in anthocyanin biosynthesis and <ce:italic>LlDFRc</ce:italic> exerted the strongest promoting effect on anthocyanin accumulation. According to the correlation analysis results, <ce:italic>LlbHLH12</ce:italic> exhibited the strongest negative correlation with <ce:italic>LlDFRc</ce:italic>. Quantitative real-time PCR analysis showed that <ce:italic>LlbHLH12</ce:italic> was highly expressed during the medium bud and full bloom stages of flower development. LlbHLH12 was identified as a member of subgroup XII of bHLH transcription factor family. Subcellular localization and transcriptional activation ability assay revealed that LlbHLH12 was located in the nucleus without transcriptional activation activity. Overexpression of <ce:italic>LlbHLH12</ce:italic> in <ce:italic>Nicotiana tabacum</ce:italic> and <ce:italic>L. longituba</ce:italic> inhibited anthocyanin accumulation by suppressing the expression of anthocyanin biosynthetic pathway genes. Furthermore, yeast one-hybrid, dual-luciferase, and <ce:italic>β</ce:italic>-glucuronidase activity assays showed that LlbHLH12 directly bound to the promoters of <ce:italic>LlPAL</ce:italic> and <ce:italic>LlDFRc</ce:italic> and suppressed their expression to inhibit anthocyanin biosynthesis. Overall, our study identified a novel bHLH repressor negatively regulating anthocyanin biosynthesis and provided new insights into the molecular mechanisms underlying color fading in <ce:italic>L. longituba</ce:italic> petals.","PeriodicalId":13178,"journal":{"name":"Horticultural Plant Journal","volume":"5 1","pages":""},"PeriodicalIF":5.7,"publicationDate":"2024-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142889400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Heat stress increases mutation efficiency mediated by CRISPR/Cas9 in citrus 热胁迫增加柑橘中CRISPR/Cas9介导的突变效率
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-21 DOI: 10.1016/j.hpj.2024.07.008
Aihong Peng, Zhiyi Chen, Yulong Zhu, Zhitan Ye, Xiuping Zou, Yongrui He, Qiang Li, Li Cao, Shanchun Chen
The CRISPR/Cas9 system has shown great promise in engineering targeted mutations in a genome. The efficiency of Cas9-mediated genome editing is temperature sensitive. A high-temperature regime can increase the mutation efficiency induced by the CRISPR/Cas9 system in many plant species. However, a heat stress treatment has not been applied during the tissue culture process in citrus. To develop an efficient heat stress regime to improve the efficiency of CRISPR/Cas9-mediated targeted mutagenesis, three and five cycles of heat stress treatments were used during callus induction in citrus. The results showed that the heat stress treatment with three cycles of 24 h at 37 °C, followed by 24 h at 26 °C, increased the mutation efficiency by 11.6 % compared with no heat stress treatment, and that five cycles of heat stress treatment were optimal, from which 50 % mutants had a 100 % mutation rate. The mutation profiles of Cas9 at 28 °C for 10 d and 37 °C for three or five cycles were similar, indicating that heat stress treatment did not affect the non-homologous end joining repair pathway. No detectable off-target mutation was detected in the potential off-target sites with four nucleotide mismatches compared with the designed on-target site. This study demonstrated that five cycles of heat stress treatment during callus induction could efficiently increase the mutation efficiency mediated by the CRISPR/Cas9 system without observable negative effects, and provided an efficient Cas9-mediated citrus genome editing system to produce mutants with a high mutation rate.
CRISPR/Cas9系统在基因组的靶向突变工程中显示出巨大的希望。cas9介导的基因组编辑效率对温度敏感。高温环境可以提高CRISPR/Cas9系统在许多植物物种中诱导的突变效率。然而,热胁迫处理在柑橘组织培养过程中尚未得到应用。为了建立一种有效的热胁迫机制来提高CRISPR/ cas9介导的靶向诱变效率,在柑橘愈伤组织诱导过程中使用了3和5个热胁迫处理周期。结果表明,37℃下24 h和26℃下24 h的3次热胁迫处理,与不进行热胁迫处理相比,突变效率提高了11.6%,其中5次热胁迫处理效果最佳,其中50%的突变体突变率为100%。Cas9在28°C处理10 d和37°C处理3或5个周期的突变谱相似,表明热应激处理不影响非同源末端连接修复途径。与设计的靶位点相比,在具有4个核苷酸错配的潜在靶位点未检测到可检测的脱靶突变。本研究表明,在愈伤组织诱导过程中,5个周期的热胁迫处理可以有效提高CRISPR/Cas9系统介导的突变效率,且无明显的负面影响,为Cas9介导的柑橘基因组编辑系统产生高突变率的突变体提供了有效的途径。
{"title":"Heat stress increases mutation efficiency mediated by CRISPR/Cas9 in citrus","authors":"Aihong Peng, Zhiyi Chen, Yulong Zhu, Zhitan Ye, Xiuping Zou, Yongrui He, Qiang Li, Li Cao, Shanchun Chen","doi":"10.1016/j.hpj.2024.07.008","DOIUrl":"https://doi.org/10.1016/j.hpj.2024.07.008","url":null,"abstract":"The CRISPR/Cas9 system has shown great promise in engineering targeted mutations in a genome. The efficiency of Cas9-mediated genome editing is temperature sensitive. A high-temperature regime can increase the mutation efficiency induced by the CRISPR/Cas9 system in many plant species. However, a heat stress treatment has not been applied during the tissue culture process in citrus. To develop an efficient heat stress regime to improve the efficiency of CRISPR/Cas9-mediated targeted mutagenesis, three and five cycles of heat stress treatments were used during callus induction in citrus. The results showed that the heat stress treatment with three cycles of 24 h at 37 °C, followed by 24 h at 26 °C, increased the mutation efficiency by 11.6 % compared with no heat stress treatment, and that five cycles of heat stress treatment were optimal, from which 50 % mutants had a 100 % mutation rate. The mutation profiles of Cas9 at 28 °C for 10 d and 37 °C for three or five cycles were similar, indicating that heat stress treatment did not affect the non-homologous end joining repair pathway. No detectable off-target mutation was detected in the potential off-target sites with four nucleotide mismatches compared with the designed on-target site. This study demonstrated that five cycles of heat stress treatment during callus induction could efficiently increase the mutation efficiency mediated by the CRISPR/Cas9 system without observable negative effects, and provided an efficient Cas9-mediated citrus genome editing system to produce mutants with a high mutation rate.","PeriodicalId":13178,"journal":{"name":"Horticultural Plant Journal","volume":"319 1","pages":""},"PeriodicalIF":5.7,"publicationDate":"2024-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142889001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Optimal combination of substrate supply amount coupled with nutrient solution management program for cucumber planting 黄瓜栽培基质用量与营养液管理方案的最优组合
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-18 DOI: 10.1016/j.hpj.2024.05.016
Zhen Kang, Zhaoxi Jiang, Zhaolong Liu, Peng Wang, Caihong Zhang, Maozhou Yuan, Mengqi Bai, Xiaohui Hu
Substrate and nutrient supply are essential for vegetable cultivation in greenhouse. The strategies for plant nutrient supply vary depending on the cultivation methods or substrate dosages employed. With the development of mechanization, wide-row spacing substrate cultivation became an optimize mode of the greenhouse cucumber cultivation, aligning with the trend of intelligent agriculture. To determine the optimal nutrient solution supply amount (NS) and supply frequency (SF) for promoting the integrated growth of cucumber under wide-row spacing substrate cultivation, we explored the effects of substrate supply amount (SS), NS, and SF on cucumber yield, quality, and element utilization efficiency. A five-level quadratic orthogonal rotation combination design with three experimental factors (NS, SF, and SS) was implemented for 23 coupling treatments over three growing seasons, including spring (2022S and 2023S) and autumn (2022A). The technique for order preference by similarity to ideal solution (TOPSIS) combining weights based on game theory was applied to construct cucumber comprehensive growth evaluation model. Single and two experimental factors analyses revealed significant effects of single factors and the coupling of NS−SS, NS−SF and SS−SF on the integrated growth of cucumber for all three growing seasons. For the NS−SF−SS combination, the optimal parameters for comprehensive cucumber growth were determined as follows: levels of −1.68 for NS, −0.7 for SF, and −1.682 for SS in 2022A; −0.43 for NS, −0.06 for SF, and 0.34 for SS in 2022S; 0.3 for NS, −0.02 for SF, and 0.04 for SS in 2023S. Furthermore, for SS ranges of 2.00–3.01, 3.01–4.50, 4.50–5.99, 5.99–7.00 (L · plant−1), the corresponding NS and SF intervals maximizing cucumber integrated growth in spring were: 0.28–0.30 (L · plant−1) and 6 (times · d−1), 0.26–0.30 (L · plant−1) and 6 (times · d−1), 0.25–0.30 (L · plant−1) and 6 (times · d−1), 0.23–0.30 (L · plant−1) and 6 (times · d−1), respectively. With the same SS, the corresponding NS and SF intervals that maximized cucumber integrated growth in autumn were: 0.10 (L · plant−1) and 8 (times · d−1), 0.18 (L · plant−1) and 7 (times · d−1), 0.30 (L · plant−1) and 6 (times · d−1), 0.49 (L · plant−1) and 5 (times · d−1), respectively. The results provide a theoretical basis for solution management, and further in-depth research on cucumber cultivation.
在温室蔬菜栽培中,基质和养分供应是至关重要的。植物养分供应的策略取决于所采用的栽培方法或基质剂量。随着机械化的发展,宽行距基质栽培成为温室黄瓜栽培的优化模式,顺应了智能化农业的发展趋势。为确定促进宽行距基质栽培下黄瓜综合生长的最佳营养液供应量(NS)和供应频率(SF),探讨了基质供应量(SS)、NS和SF对黄瓜产量、品质和元素利用效率的影响。采用3个试验因子(NS、SF和SS)的5水平二次正交旋转组合设计,在春季(2022S和2023S)和秋季(2022A) 3个生长季节进行23个耦合处理。采用基于博弈论的TOPSIS (order preference by similarity by ideal solution)组合权重法构建黄瓜综合生长评价模型。单因素和双因素试验分析表明,单因素和NS - SS、NS - SF和SS - SF的耦合对黄瓜3个生长季节的综合生长均有显著影响。以NS - SF - SS组合为例,在2022A条件下,NS - 1.68、SF - 0.7、SS - 1.682为黄瓜综合生长的最佳水平;2022S中,NS为- 0.43,SF为- 0.06,SS为0.34;2023S NS为0.3,SF为−0.02,SS为0.04。在SS为2.00-3.01、3.01-4.50、4.50-5.99、5.99-7.00 (L·株−1)范围内,春季黄瓜综合生长最大化的NS和SF区间分别为:0.28-0.30 (L·株−1)和6(次·d−1)、0.26-0.30 (L·株−1)和6(次·d−1)、0.25-0.30 (L·株−1)和0.23-0.30 (L·株−1)和6(次·d−1)。在相同SS条件下,秋季黄瓜综合生长最大的NS和SF间隔分别为:0.10 (L·株−1)和8(次·d−1)、0.18 (L·株−1)和7(次·d−1)、0.30 (L·株−1)和6(次·d−1)、0.49 (L·株−1)和5(次·d−1)。研究结果为溶液管理和黄瓜栽培的进一步深入研究提供了理论依据。
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引用次数: 0
Establishment of an in vivo transgenic hairy root system in strawberry for verifying the nitrate-transport activity of FaNRT1.1 在草莓中建立转基因毛状根系,验证FaNRT1.1的硝酸盐转运活性
IF 5.7 1区 农林科学 Q1 HORTICULTURE Pub Date : 2024-12-18 DOI: 10.1016/j.hpj.2024.11.001
Fuling Hao, Sixin Wu, Zhongyuan Shen, Maoting Tang, Xiangjun Ge, Muqian Wu, Qihan Sun, Congbing Fang
The study of strawberry gene function has been hindered by the low transformation efficiency and long generation time of transgenic plants. This study aimed to develop and optimize methods for generating strawberry (Fragaria × ananassa Duch. ‘Benihoppe’) plants with transgenic hairy roots. This involved inducing hairy roots on strawberry stolons near new plants, optimizing several parameters that affect the survival rate of stolon hairy roots, and using the new hairy root transgenic system to investigate the nitrate-transport function of FaNRT1.1. In vivo injection (IVI) of Agrobacterium rhizogenes K599 (OD600 = 1.0) at sites measuring 0.5–1 cm on the tops of mature stolons (9–12 days old) of ‘Benihoppe’ strawberry resulted in the establishment of strawberries with transgenic hairy roots. The IVI induced epidermal bulges and hairy roots in 50 % of the stolons. The epidermal bulges were evident, and callus began to grow 35 days post-injection, while hairy roots began to develop near the injection sites at 40 days and became abundant by 60 days. Specific fluorescence signals were observed in all transgenic hairy roots of 40 new plants. Using 15N nitrate labeling, we confirmed the nitrate-transport—from roots to shoots—function of FaNRT1.1 in the strawberry plants with transgenic hairy roots. Taken together, sufficient hairy roots can be induced using an efficient transgenic hairy root system, which can be effectively applied to gene function research, such as the analysis of the nitrate-transport activity of FaNRT1.1.
草莓基因功能的研究一直受到转基因植株转化效率低、世代长等问题的制约。本研究旨在开发和优化草莓(Fragaria × ananassa Duch)的生产工艺。‘ Benihoppe ’)具有转基因毛状根的植物。这包括在新植株附近的草莓匍匐茎上诱导毛状根,优化影响匍匐茎毛状根成活率的几个参数,并利用新的毛状根转基因系统研究FaNRT1.1的硝酸盐转运功能。在‘Benihoppe’草莓成熟匍匐茎(9-12 d)顶部0.5-1 cm的位置体内注射根生农杆菌K599 (OD600 = 1.0),可获得转基因毛状根草莓。IVI诱导50%的匍匐茎出现表皮隆起和毛状根。注射后35 d,表皮明显隆起,愈伤组织开始生长;注射后40 d,毛状根在注射部位附近开始发育,60 d时毛状根数量增多。在40株新植株的毛状根中均观察到特异性荧光信号。利用15N硝酸盐标记技术,证实了转基因毛状根草莓植株中FaNRT1.1基因的硝酸盐从根到茎的转运功能。综上所述,利用高效的转基因毛状根系可以诱导出足够的毛状根,可以有效地应用于基因功能研究,如分析FaNRT1.1的硝酸盐转运活性。
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引用次数: 0
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Horticultural Plant Journal
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